The Role of ctDNA Testing Plus AI-based Pathology in Resectable LSCC

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-75
SponsorSecond Xiangya Hospital of Central South University

About this trial

The goal of this observational study is to explore whether ctDNA dynamic monitoring plus AI-based pathology can more effectively predict the therapeutic effect of neoadjuvant chemoimmunotherapy for resectable lung squamous cell carcinoma, so as to accurately guide clinical diagnosis and treatment.

Eligibility criteria

Qualifiers

Histopathology or cytology confirmed the lung squamous cell carcinoma

Age ranging from 18 to 75

Agree to participate in this study and sign an informed consent form

Treatment-naive tumor

Disqualifiers

Patients who cannot understand the content of the experiment and cannot cooperate, and those who refuse to sign the informed consent form

Non-squamous NSCLC

Unresectable IIIa-IIIb tumor

Patients with solid organ or blood system transplantation

Trial design

Treatments tested in this trial

  • WES and ctDNA detection

Treatment groups

50 Participants
are divided into 1 treatment group

Sponsors and collaborators